Allele Registry

Canonical Allele Identifier: PA2825839012

Gene: RNASEH2B HGNC NCBI

ClinVar RCV:

RCV002009665

ClinVar Variation:

1508096

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135751.1:p.Tyr219His	CA249998464 NM_001142279.2:c.655T>C